Canonical Allele Identifier: CA1331555919
Gene: CUL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503651C= , CM000664.2:g.224503651C= GRCh38
NC_000002.11:g.225368368C= , CM000664.1:g.225368368C= GRCh37
NC_000002.10:g.225076612C= NCBI36
NG_032169.1:g.86747G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264414.9:c.1377+1G= MANE Select ENSP00000264414.4:n.1377+1G=
ENST00000264414.8:c.1377+1G= ENSP00000264414.4:n.1377+1G=
ENST00000344951.8:c.1179+1G= ENSP00000343601.4:n.1179+1G=
ENST00000409096.5:c.1305+1G= ENSP00000387200.1:n.1305+1G=
ENST00000409777.5:c.1305+1G= ENSP00000386525.1:n.1305+1G=
ENST00000481135.1:n.673+1G=
ENST00000617432.4:c.99+1G= ENSP00000477851.1:n.99+1G=
NM_001257197.1:c.1179+1G= NP_001244126.1:n.1179+1G=
NM_001257198.1:c.1395+1G= NP_001244127.1:n.1395+1G=
NM_003590.4:c.1377+1G= NP_003581.1:n.1377+1G=
XM_006712800.2:c.1344+1G= XP_006712863.2:n.1344+1G=
XM_011511994.1:c.1230+1G= XP_011510296.1:n.1230+1G=
XM_011511995.1:c.1335+1G= XP_011510297.1:n.1335+1G=
XM_011511996.1:c.1185+1G= XP_011510298.1:n.1185+1G=
XM_011511997.1:c.1077+1G= XP_011510299.1:n.1077+1G=
XM_011511994.3:c.1230+1G= XP_011510296.1:n.1230+1G=
XM_011511996.2:c.1185+1G= XP_011510298.1:n.1185+1G=
NM_003590.5:c.1377+1G= MANE Select NP_003581.1:n.1377+1G=
NM_001257198.2:c.1395+1G= NP_001244127.1:n.1395+1G=
NM_001257197.2:c.1179+1G= NP_001244126.1:n.1179+1G=